Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes.

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Human Heredity Pub Date : 2018-01-01 Epub Date: 2019-05-27 DOI:10.1159/000496867
Youfei Yu, Lu Xia, Seunggeun Lee, Xiang Zhou, Heather M Stringham, Michael Boehnke, Bhramar Mukherjee
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引用次数: 8

Abstract

Objectives: Classical methods for combining summary data from genome-wide association studies only use marginal genetic effects, and power can be compromised in the presence of heterogeneity. We aim to enhance the discovery of novel associated loci in the presence of heterogeneity of genetic effects in subgroups defined by an environmental factor.

Methods: We present a pvalue-assisted subset testing for associations (pASTA) framework that generalizes the previously proposed association analysis based on subsets (ASSET) method by incorporating gene-environment (G-E) interactions into the testing procedure. We conduct simulation studies and provide two data examples.

Results: Simulation studies show that our proposal is more powerful than methods based on marginal associations in the presence of G-E interactions and maintains comparable power even in their absence. Both data examples demonstrate that our method can increase power to detect overall genetic associations and identify novel studies/phenotypes that contribute to the association.

Conclusions: Our proposed method can be a useful screening tool to identify candidate single nucleotide polymorphisms that are potentially associated with the trait(s) of interest for further validation. It also allows researchers to determine the most probable subset of traits that exhibit genetic associations in addition to the enhancement of power.

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利用基因-环境相互作用发现跨多种研究或表型的遗传关联的基于子集的分析。
目的:结合全基因组关联研究汇总数据的经典方法仅使用边际遗传效应,并且在存在异质性的情况下,能力可能会受到损害。我们的目标是加强在由环境因素定义的亚群中存在遗传效应异质性的新相关位点的发现。方法:我们提出了一个价值辅助的关联子集测试(pASTA)框架,该框架通过将基因-环境(G-E)相互作用纳入测试过程,推广了先前提出的基于子集(ASSET)方法的关联分析。我们进行了仿真研究,并提供了两个数据示例。结果:模拟研究表明,我们的建议比基于边际关联的方法在存在G-E相互作用的情况下更强大,即使在没有它们的情况下也能保持相当的能力。这两个数据示例表明,我们的方法可以提高检测整体遗传关联的能力,并确定有助于关联的新研究/表型。结论:我们提出的方法可以作为一种有用的筛选工具,用于鉴定候选单核苷酸多态性,这些多态性可能与感兴趣的性状相关,以便进一步验证。它还使研究人员能够确定除了力量增强外,最可能表现出遗传关联的特征子集。
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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